3705-27-9
Chemical Structure
Cyclo(Gly-L-Pro)
- CAS No.: 3705-27-9
- Formula:C7H10N2O2
- Molecular Weight:154.17
IUPAC Name: (S)-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione
InChIKey: OWOHLURDBZHNGG-YFKPBYRVSA-N
SMILES: O=C1[C@@]2([H])N(CCC2)C(CN1)=O
Biological Activity: Cyclo(Gly-L-Pro) is a Alkaloids product that can be isolated from the roots of Panax notoginseng (Burk.)F.H.Chen[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Cyclo(Gly-L-Pro) | 99.93% | Cyclo(Gly-L-Pro) is a Alkaloids product that can be isolated from the roots of Panax notoginseng (Burk.)F.H.Chen. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Cyclo(Gly-Pro) | Cyclo(Gly-Pro) is a cyclic dipeptide. Cyclo(Gly-Pro) exerts analgesic effects through opioid receptor-related pathways and reduces IFN-γ-induced cellular cytokine/chemokine biomarkers. Cyclo(Gly-Pro) inhibits induced nociception in mouse models, reduces carrageenan- and other inducer-induced paw edema and myeloperoxidase in inflamed paws, and increases the number of c-Fos-positive neurons in the midbrain periaqueductal gray. Cyclo(Gly-Pro) can be used in research related to pain and inflammatory diseases. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
-
Similarity Score 1.00
HY-W062171RCyclo-(Pro-Gly) (Standard) -
Similarity Score 0.84
HY-N10185Cyclo(D-Ala-L-Pro) -
Similarity Score 0.84
HY-P1935Cyclo(Ala-Pro) -
Similarity Score 0.78
HY-N11615Cyclo(Pro-Val) -
Similarity Score 0.78
HY-N11615A(R,R)-Cyclo(Pro-Val) -
Similarity Score 0.78
HY-N14562Cyclo (D-Pro-L-Val) -
Similarity Score 0.78
HY-P1938RCyclo(L-Pro-L-Val) (Standard) -
Similarity Score 0.78
HY-W942561Cyclo(D-Val-L-Pro) -
Similarity Score 0.77
HY-P5050Cyclo(Pro-Thr) -
Explore the MedChemAI to find more analogs